GB1120210A - Thiazole derivatives - Google Patents
Thiazole derivativesInfo
- Publication number
- GB1120210A GB1120210A GB46150/65A GB4615065A GB1120210A GB 1120210 A GB1120210 A GB 1120210A GB 46150/65 A GB46150/65 A GB 46150/65A GB 4615065 A GB4615065 A GB 4615065A GB 1120210 A GB1120210 A GB 1120210A
- Authority
- GB
- United Kingdom
- Prior art keywords
- formula
- cyclopropyl
- compounds
- derivatives
- thiazole
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 150000007979 thiazole derivatives Chemical class 0.000 title abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 7
- -1 chloro- Chemical class 0.000 abstract 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000000203 mixture Substances 0.000 abstract 3
- 229910052794 bromium Inorganic materials 0.000 abstract 2
- 229910052801 chlorine Inorganic materials 0.000 abstract 2
- 239000000460 chlorine Substances 0.000 abstract 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 2
- 229910052740 iodine Inorganic materials 0.000 abstract 2
- BRMYZIKAHFEUFJ-UHFFFAOYSA-L mercury diacetate Chemical compound CC(=O)O[Hg]OC(C)=O BRMYZIKAHFEUFJ-UHFFFAOYSA-L 0.000 abstract 2
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 abstract 2
- UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract 2
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 abstract 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical group [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 239000004150 EU approved colour Substances 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000007513 acids Chemical class 0.000 abstract 1
- 230000010933 acylation Effects 0.000 abstract 1
- 238000005917 acylation reaction Methods 0.000 abstract 1
- 239000000654 additive Substances 0.000 abstract 1
- 239000000853 adhesive Substances 0.000 abstract 1
- 230000001070 adhesive effect Effects 0.000 abstract 1
- 125000001931 aliphatic group Chemical group 0.000 abstract 1
- 229910001514 alkali metal chloride Inorganic materials 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 150000001558 benzoic acid derivatives Chemical class 0.000 abstract 1
- 150000008359 benzonitriles Chemical class 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 1
- 230000007797 corrosion Effects 0.000 abstract 1
- 238000005260 corrosion Methods 0.000 abstract 1
- 239000002274 desiccant Substances 0.000 abstract 1
- 150000004891 diazines Chemical class 0.000 abstract 1
- 239000003085 diluting agent Substances 0.000 abstract 1
- 239000002270 dispersing agent Substances 0.000 abstract 1
- 230000000694 effects Effects 0.000 abstract 1
- 239000003995 emulsifying agent Substances 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 230000026030 halogenation Effects 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 230000002363 herbicidal effect Effects 0.000 abstract 1
- 230000007062 hydrolysis Effects 0.000 abstract 1
- 238000006460 hydrolysis reaction Methods 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 239000003112 inhibitor Substances 0.000 abstract 1
- 239000011630 iodine Chemical group 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- 229960002523 mercuric chloride Drugs 0.000 abstract 1
- LWJROJCJINYWOX-UHFFFAOYSA-L mercury dichloride Chemical compound Cl[Hg]Cl LWJROJCJINYWOX-UHFFFAOYSA-L 0.000 abstract 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 125000001453 quaternary ammonium group Chemical class 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 239000004094 surface-active agent Substances 0.000 abstract 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 abstract 1
- 150000003918 triazines Chemical class 0.000 abstract 1
- 150000003852 triazoles Chemical class 0.000 abstract 1
- 150000003672 ureas Chemical class 0.000 abstract 1
- 238000009736 wetting Methods 0.000 abstract 1
- 239000000080 wetting agent Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P13/00—Preparation of nitrogen-containing organic compounds
- C12P13/04—Alpha- or beta- amino acids
- C12P13/06—Alanine; Leucine; Isoleucine; Serine; Homoserine
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D277/32—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D277/38—Nitrogen atoms
- C07D277/44—Acylated amino or imino radicals
- C07D277/46—Acylated amino or imino radicals by carboxylic acids, or sulfur or nitrogen analogues thereof
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Zoology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Microbiology (AREA)
- General Chemical & Material Sciences (AREA)
- Biotechnology (AREA)
- Health & Medical Sciences (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Genetics & Genomics (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB46150/65A GB1120210A (en) | 1965-11-01 | 1965-11-01 | Thiazole derivatives |
| NL6615037A NL6615037A (enrdf_load_stackoverflow) | 1965-11-01 | 1966-10-24 | |
| US590181A US3468899A (en) | 1965-11-01 | 1966-10-28 | Thiazole derivatives |
| DE1542977A DE1542977B2 (de) | 1965-11-01 | 1966-10-31 | Thiazolderivate, Verfahren zu ihrer Herstellung und herbicide Mittel |
| BE689108D BE689108A (enrdf_load_stackoverflow) | 1965-11-01 | 1966-10-31 | |
| CH1579766A CH467577A (fr) | 1965-11-01 | 1966-11-01 | Composition herbicide |
| FR82241A FR1499577A (fr) | 1965-11-01 | 1966-11-02 | Procédé de préparation de la l-sérine par fermentation |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB46150/65A GB1120210A (en) | 1965-11-01 | 1965-11-01 | Thiazole derivatives |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1120210A true GB1120210A (en) | 1968-07-17 |
Family
ID=10440053
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB46150/65A Expired GB1120210A (en) | 1965-11-01 | 1965-11-01 | Thiazole derivatives |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US3468899A (enrdf_load_stackoverflow) |
| BE (1) | BE689108A (enrdf_load_stackoverflow) |
| CH (1) | CH467577A (enrdf_load_stackoverflow) |
| DE (1) | DE1542977B2 (enrdf_load_stackoverflow) |
| FR (1) | FR1499577A (enrdf_load_stackoverflow) |
| GB (1) | GB1120210A (enrdf_load_stackoverflow) |
| NL (1) | NL6615037A (enrdf_load_stackoverflow) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4046753A (en) * | 1973-10-11 | 1977-09-06 | Merck & Co., Inc. | Substituted 2-phenylhydrazino and 2-phenylazo thiazolines |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3002024A (en) * | 1957-03-12 | 1961-09-26 | Goodrich Co B F | Bis-ketenes and method of preparation |
| US3215727A (en) * | 1961-04-24 | 1965-11-02 | Phillips Petroleum Co | Esters and acids useful as additives and method of preparation |
| US3277107A (en) * | 1962-03-16 | 1966-10-04 | Gulf Oil Corp | Cyclopropanecarboxamide and cyclopropanethiocarboxamide derivatives |
| US3374082A (en) * | 1965-01-25 | 1968-03-19 | Upjohn Co | Herbicidal methods and compositions comprising 2-amino and lower alkanoamido-5-halothiazoles |
-
1965
- 1965-11-01 GB GB46150/65A patent/GB1120210A/en not_active Expired
-
1966
- 1966-10-24 NL NL6615037A patent/NL6615037A/xx unknown
- 1966-10-28 US US590181A patent/US3468899A/en not_active Expired - Lifetime
- 1966-10-31 DE DE1542977A patent/DE1542977B2/de active Pending
- 1966-10-31 BE BE689108D patent/BE689108A/xx unknown
- 1966-11-01 CH CH1579766A patent/CH467577A/fr unknown
- 1966-11-02 FR FR82241A patent/FR1499577A/fr not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| BE689108A (enrdf_load_stackoverflow) | 1967-05-02 |
| NL6615037A (enrdf_load_stackoverflow) | 1967-05-02 |
| US3468899A (en) | 1969-09-23 |
| FR1499577A (fr) | 1967-10-27 |
| CH467577A (fr) | 1969-01-31 |
| DE1542977A1 (de) | 1970-07-16 |
| DE1542977B2 (de) | 1975-08-07 |
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